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pAxCAwtit

A dual cassette for constructing recombinant adenovirus containing CAG promoter

Catalog number RDB03121
Resource name pAxCAwtit
Clone info. A dual cassette for constructing recombinant adenovirus containing CAG promoter improved from pAxCAwt. Please note that pAxCAwtit has been improved as pAxCAwtit2 (RDB05213), which contains a Csp45I site and an additional PacI site for linearizing the cosmid vector by restriction enzymes.
Comment The pAxCAwtit cosmid is a derivative of pAxcwit (RDB 3120) and can be used to clone a CAG cassette [Niwa et al., Gene 108, 193-99, 1991], harboring a unique SwaI site as the cloning site for the gene of interest, at the E1 deletion. Upon transfection of HEK293 cells, the pAxCAwtit cosmid, digested with Csp45I, can generate rAd. The pAxCAwtit cosmid can also be used to generate rAd by the COS-TPC method [Miyake et al., Proc. Natl. Acad. Sci. USA 93, 1320-24, 1996].
Vector backbone charomid 9-11 (Cosmid, use packaging extracts for transformation)
Size of vector backbone 11 kb
Selectable markers Amp^r
Gene/insert name AdV_5 E1, E3-deleted adenovirus 5 genome Genomic DNA
Depositor|Developer Saito, Izumu |
Other clones in our bank
External Database
AdV_5 E1, E3-deleted adenovirus 5 genome
            Reference sequence
              

            Distribution information

            Please check terms and conditions set forth by the depositor, which are specified in the RIKEN BRC Catalog and/or Web Catalog.
            Terms and conditions set forth by the DEPOSITOR In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of literature designated by the DEPOSITOR is requested (Terashima, M., Exp. Med., 21, 931-936(2003)).
            Additional terms and conditions for distribution Regarding resources containing CAG promoter: In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation for the CAG promoter (Niwa, H., Yamamura, K., Miyazaki, J., Gene 108 : 193-200, 1991) and an acknowledgment to Dr. Jun-ich Miyazaki of the Osaka University are requested.
            Ordering Please visit Information of Request for Distribution.[link] For for-profit-research purpose, please contact us. 
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            Material Transfer Agreement (MTA for use for not-for-profit academic purpose) [Word]
            Remarks Remember that you will be working with samples containing infectious virus.
            提供案内 (日本国内) [open/close]

            提供条件 利用者は、研究成果の公表にあたって寄託者の指定する文献を引用する (Terashima, M., Exp. Med., 21, 931-936(2003))。
            付加的提供条件 CAGプロモータを含むリソースについて: 利用者は、研究成果の公表にあたってCAGプロモータの文献 (Niwa, H., Yamamura, K., Miyazaki, J., Gene 108 : 193-200, 1991)を引用し、大阪大学 宮崎純一博士への謝辞の表明を必要とする。
            提供依頼 手続きの詳細は、「提供申込みについて[link]」をご覧ください。営利目的利用についてはお問い合わせください。
            提供依頼書 [Word]
            提供同意書 (MTA、非営利機関による非営利学術研究用)[Word]
            備考 このリソースはウイルス粒子産生用のため、取扱いに注意が必要です。

            Catalog # Resource name Availability Shipping form Fee (non-profit org.)
            RDB03121 pAxCAwtit Under QC test. Please contact us. DNA solution

            check Please wait for results of QC test to be uploaded. This clone will be sequenced a portion for examination.

            References and tips

            Electronic file

            Sequence RDB03121u.seq
            Sequence RDB03121v.seq
            Sequence RDB03121w.seq
            Sequence RDB03121x.seq
            Sequence RDB03121y.seq
            Sequence RDB03121z.seq
            Remarks, protocol and/or map (gif) RDB03121.gif
            Remarks, protocol and/or map (pdf) RDB03121.pdf

            Original reference

            original Fukuda, H., Possible mechanism of adenovirus generation from a cloned viral genome tagged with nucleotides at its ends. Microbiol. Immunol., 50, 643-654 (2006). PMID 16924150.
            original Terashima, M., [Japanese text] Exp. Med., 21, 931-936 (2003).

            Further references such as user reports and related articles (go to bottom)

            Featured content

            Sequence information

            check Please wait for results of QC test to be uploaded. This clone will be sequenced a portion for examination.

            References

            Original, user report and related articles

            original Fukuda, H., Possible mechanism of adenovirus generation from a cloned viral genome tagged with nucleotides at its ends. Microbiol. Immunol., 50, 643-654 (2006). PMID 16924150.
            original Terashima, M., [Japanese text] Exp. Med., 21, 931-936 (2003).
            user_report Heng, J.I., The zinc finger transcription factor RP58 negatively regulates Rnd2 for the control of neuronal migration during cerebral cortical development. Cereb. Cortex 25 (3): 806-816 (2015). PMID 24084125.
            user_report Ikeno Y., Secretory phospholipases A2 induce neurite outgrowth in PC12 cells through lysophosphatidylcholine generation and activation of G2A receptor. J. Biol. Chem., 280, 28044-28052, (2005). PMID 15927955.

            2022.05.18

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